Levetiracetam

Phase 2Completed
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Interest: 35/100
35
Hype Score

Development Stage

Pre-clinical
Phase 1
3
Phase 2
4
Phase 3
5
Approved
Indication / Disease

Motor Neuron Disease

Conditions

Motor Neuron Disease, Amyotrophic Lateral Sclerosis, Primary Lateral Sclerosis, Progressive Muscular Atrophy

Trial Timeline

May 1, 2006 → Jun 1, 2008

About Levetiracetam

Levetiracetam is a phase 2 stage product being developed by UCB for Motor Neuron Disease. The current trial status is completed. This product is registered under clinical trial identifier NCT00324454. Target conditions include Motor Neuron Disease, Amyotrophic Lateral Sclerosis, Primary Lateral Sclerosis.

Hype Score Breakdown

Clinical
12
Activity
8
Company
15
Novelty
0
Community
0

Clinical Trials (20)

NCT IDPhaseStatus
NCT03340064Phase 3Completed
NCT01618877Phase 1Completed
NCT01407523Phase 2Completed
NCT01398956Phase 3Completed
NCT01292837Phase 3Completed
NCT01063764Phase 3Completed
NCT00505934Phase 2Completed
NCT00627133Phase 2Withdrawn
NCT00535392Phase 2Completed
NCT00376766Phase 3Terminated
NCT00361010Pre-clinicalCompleted
NCT01318408ApprovedCompleted
NCT00367432Phase 3Completed
NCT00291655Phase 3Completed
NCT00324454Phase 2Completed
NCT00319605Pre-clinicalCompleted
NCT00307450ApprovedCompleted
NCT00279617Phase 3Completed
NCT00325182ApprovedCompleted
NCT00252954ApprovedCompleted

Competing Products

20 competing products in Motor Neuron Disease

See all competitors
ProductCompanyStageHype Score
fezolinetant + placeboAstellas PharmaPhase 3
40
Ranirestat + PlaceboEisaiPhase 2/3
38
Raloxifene + medroxyprogesterone acetate + estrogen + 17 beta estradiolEli LillyPhase 2
35
APL-130277 + subcutaneous apomorphineSumitomo PharmaPhase 3
40
esomeprazole + placeboAstraZenecaPre-clinical
26
MK-6913 + 17-β estradiol + Placebo to MK-6913 + Placebo to 17-β estradiol + MK-6913 25 mgMerckPhase 2
27
Erenumab + PlaceboAmgenPhase 1
29
17B Estradiol (1mg) / (0.125 mg) TMG Continuous combined (Totelle) + Tibolone (Livial)PfizerApproved
43
DVS-233 SRPfizerPhase 3
40
1 mg QD to 15 mg QD PF-06649751 + 3 mg QD to 15 mg QD PF-06649751 + 7 mg QD to 15 mg QD PF-06649751 + 15 mg QD PF-06649751 + 1 mg QD to 7 mg QD PF-06649751 (if de-escalated in parent study) + 3 mg QD to 7 mg QD PF-06649751 (de-escalated in parent study) + 7 mg QD to 7 mg QD PF-06649751 (de-escalated in parent study) + 15 mg QD de-escalated to 7 mg QD PF-06649751 in parent study remain at 7 mg QDPfizerPhase 2
27
Bazedoxifene/Conjugated EstrogenPfizerPhase 3
40
desvenlafaxine succinate sustained release (DVS SR)PfizerPhase 1
29
desvenlafaxine succinate sustained release + desvenlafaxine succinate sustained release + desvenlafaxine succinate sustained release + desvenlafaxine succinate sustained release + Placebo + desvenlafaxine succinate sustained release + desvenlafaxine succinate sustained release + desvenlafaxine succinate sustained releasePfizerPhase 3
40
desvenlafaxine succinate (DVS) SR + PlaceboPfizerPhase 3
40
VivaglobinCSLPhase 2
35
ARGX-117ArgenxPhase 2
36
Empasiprubart + IVIG (Intravenous Immunoglobulin)ArgenxPhase 3
44
ARGX-117ArgenxPhase 2
32
Treatment A + Treatment B + Treatment CBayerPhase 1
26
Elinzanetant (BAY3427080) + PlaceboBayerPhase 1
26